Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HF57
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.744 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.525 |
CLV_PCSK_PC7_1 | 116 | 122 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.459 |
DOC_CKS1_1 | 72 | 77 | PF01111 | 0.348 |
DOC_CYCLIN_yCln2_LP_2 | 145 | 148 | PF00134 | 0.519 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.321 |
DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.506 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.529 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 102 | 109 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 216 | 222 | PF00244 | 0.477 |
LIG_APCC_ABBA_1 | 244 | 249 | PF00400 | 0.403 |
LIG_BIR_III_4 | 197 | 201 | PF00653 | 0.658 |
LIG_eIF4E_1 | 48 | 54 | PF01652 | 0.496 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.414 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.599 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.459 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.444 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.417 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.579 |
LIG_LIR_Apic_2 | 142 | 147 | PF02991 | 0.498 |
LIG_PCNA_yPIPBox_3 | 62 | 73 | PF02747 | 0.549 |
LIG_Pex14_1 | 122 | 126 | PF04695 | 0.456 |
LIG_REV1ctd_RIR_1 | 106 | 114 | PF16727 | 0.553 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.571 |
LIG_SH2_STAT3 | 209 | 212 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.572 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.703 |
LIG_SxIP_EBH_1 | 156 | 167 | PF03271 | 0.529 |
LIG_TYR_ITIM | 59 | 64 | PF00017 | 0.608 |
LIG_UBA3_1 | 53 | 62 | PF00899 | 0.554 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.540 |
LIG_WRC_WIRS_1 | 218 | 223 | PF05994 | 0.394 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.553 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.604 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.633 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.746 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.508 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.560 |
MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.481 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.524 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.515 |
MOD_GlcNHglycan | 223 | 228 | PF01048 | 0.409 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.411 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.431 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.482 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.386 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.496 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.552 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.377 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.731 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.712 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.544 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.540 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.562 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.503 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.449 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.474 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.466 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.518 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.519 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.555 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.535 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.497 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.457 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.596 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.356 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.668 |
TRG_DiLeu_BaLyEn_6 | 213 | 218 | PF01217 | 0.574 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA87 | Leptomonas seymouri | 71% | 100% |
A0A0S4J0K3 | Bodo saltans | 35% | 100% |
A0A1X0P8R4 | Trypanosomatidae | 38% | 88% |
A0A3R7JYN8 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X040 | Leishmania donovani | 79% | 100% |
A4I2E1 | Leishmania infantum | 79% | 100% |
C9ZX66 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 93% |
E9AYJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q8X9 | Leishmania major | 81% | 100% |
V5BA09 | Trypanosoma cruzi | 37% | 84% |